Adenosine A_2A receptors are required for normal BDNF levels and BDNF-induced potentiation of synaptic transmission in the mouse hippocampus

Authors: Tebano, M. T.¹; Martire, A.¹; Potenza, R. L.¹; Grò, C.¹; Pepponi, R.¹; Armida, M.¹; Domenici, M. R.¹; Schwarzschild, M. A.²; Chen, J. F.³; Popoli, P.¹

Source: Journal of Neurochemistry, Volume 104, Number 1, January 2008 , pp. 279-286(8)

Publisher: Wiley-Blackwell

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Abstract:

Brain-derived neurotrophic factor (BDNF), a member of neurotrophin family, enhances synaptic transmission and regulates neuronal proliferation and survival. Both BDNF and its tyrosine kinase receptors (TrkB) are highly expressed in the hippocampus, where an interaction with adenosine A_2A receptors (A_2ARs) has been recently reported. In the present paper, we evaluated the role of A_2ARs in mediating functional effects of BDNF in hippocampus using A_2AR knock-out (KO) mice. In hippocampal slices from WT mice, application of BDNF (10 ng/mL) increased the slope of excitatory post-synaptic field potentials (fEPSPs), an index of synaptic facilitation. This increase of fEPSP slope was abolished by the selective A_2A antagonist ZM 241385. Similarly, genetic deletion of the A_2ARs abolished BDNF-induced increase of the fEPSP slope in slices from A_2AR KO mice The reduced functional ability of BDNF in A_2AR KO mice was correlated with the reduction in hippocampal BDNF levels. In agreement, the pharmacological blockade of A₂Rs by systemic ZM 241385 significantly reduced BDNF levels in the hippocampus of normal mice. These results indicate that the tonic activation of A_2ARs is required for BDNF-induced potentiation of synaptic transmission and for sustaining a normal BDNF tone in the hippocampus.

Keywords: adenosine A2A receptors; BDNF levels; hippocampus; synaptic transmission

Document Type: Research article

DOI: http://dx.doi.org/10.1111/j.1471-4159.2007.05046.x

Affiliations: 1: Department of Therapeutic Research and Medicine Evaluation, Istituto Superiore di Sanità, Viale Regina Elena, Rome, Italy 2: MassGeneral Institute for Neurodegenerative Disease, Boston, Massachusetts, USA 3: Molecular Neuropharmacology Laboratory, Department of Neurology, Boston University School of Medicine, Boston, Massachusetts, USA

Publication date: 2008-01-01